Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CPR D & C TRAY

K-Number: K960239 · 1996-05-23

ApplicantCustom Pack Reliability
Decision Date1996-05-23
Product CodeHHK
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CPR D & C TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Custom Pack Reliability. It received FDA 510(k) clearance on 1996-05-23 under 510(k) number K960239. The device is classified under product code HHK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR D & C TRAY?

CPR D & C TRAY is a medical device that received FDA 510(k) clearance on 1996-05-23. The listed applicant is Custom Pack Reliability. The 510(k) number is K960239.

When did CPR D & C TRAY receive FDA 510(k) clearance?

CPR D & C TRAY received FDA 510(k) clearance on 1996-05-23, under 510(k) number K960239.

Who is the listed applicant for CPR D & C TRAY?

The FDA 510(k) record lists Custom Pack Reliability as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CPR D & C TRAY?

The FDA product code for CPR D & C TRAY is HHK.

Other records listing Custom Pack Reliability as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960205CPR TRACHEOTOMY CARE TRAYK960243CPR C-SECTION DELIVERY PACKK960216CPR SUCTION CATHETER KITK960213CPR TOTAL HIP PACKK960210CPR ORTHO HAND PACKK960206CPR DRESSING CHANGE TRAY

View all 21 devices →

Related Devices (Code: HHK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251882Uterine Aspiration SetGcmedica Enterprise Ltd.(Wuxi)K240434RELIEEV Suction Curette (Flexible 3.0/ Standard 3.6)Li Medical Corporation , Ltd.K201952CrossGlide ETS PlusCrossbay MedicalK192534CrossBay Endometrial Tissue Sampler (ETS)Crossbay MedicalK102847DISPOSABLE ENDOMETRIAL SUCTION CURETTEJiangsu Suyun Medical Materials Co., Ltd.K092982THE PANPAC SUCTION CURETTEPanpac Medical Corporation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑